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Thyroxine withdrawal prior to radioiodine therapy in papillary thyroid carcinoma - current scenarios.

Created on 13 Aug 2026

Authors

Saumya Sunny, Julie Hephzibah

Published in

Current opinion in endocrinology, diabetes, and obesity. Aug 13, 2026. Epub Aug 13, 2026.

Abstract

This review aims to compare the different methods of achieving adequate thyroid-stimulating hormone (TSH) stimulation prior to radioiodine (RAI) therapy in patients with differentiated thyroid carcinoma (DTC). It focuses on thyroid hormone withdrawal strategies and recombinant human TSH, examining their relative efficacy, safety, and impact on patient quality of life. Additionally, the review highlights recent guideline updates, and how these approaches influence postoperative risk stratification, treatment decision-making, and follow-up.
Emerging evidence is challenging traditional assumptions regarding optimal TSH stimulation thresholds and the necessity of prolonged thyroid hormone withdrawal, reflecting a broader shift toward individualized, risk-adapted management strategies in DTC. THW (Thyroid hormone withdrawal) delivers higher lesion doses; rhTSH (Recombinant human TSH) reduces whole-body radiation, with similar outcomes in low/intermediate-risk patients. Both achieve comparable ablation success, but rhTSH is safer and better tolerated. Both are suitable for dynamic risk stratification while rhTSH allows continued TSH suppression, aiding follow-up.
Both THW and rhTSH are effective, but modern practice is shifting toward individualized, patient-centered use of rhTSH. However, THW still remains relevant in high disease burden and resource-limited settings. Future research is focused on optimizing thresholds, clarifying its role in molecular profiling, re-differentiation, and dosimetry-guided therapies.

PMID:
42590940
Bibliographic data and abstract were imported from PubMed on 13 Aug 2026.

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